Plants grow mostly by increasing the size of cells in enlarging regions. For a cell to become larger, the wall becomes irreversibly extended by \(*P\)*. In effect, the wall in a growing cell is constructed so the polymers slip a little at high \(*P\)*. In that situation, as \(*P\)* builds from osmosis, it never reaches a level where equilibration can occur. Instead, \(*P\)* can only build enough to cause irreversible slippage (yielding) of the wall and the wall compartment becomes bigger. This can be demonstrated by lowering \(*P\)*. Even if \(*P\)* decreases as low as zero, the compartment remains bigger than it was.

Typically the \(*P\)* must be higher than a minimum before yielding occurs. It is possible to express this wall property with an equation similar to Eq. 2. Lockhart (1965) was the first to do so and described cell enlargement for \(*P\)*-driven growth as:

\[\frac{dV}{dt} = A \phi (P - P_{th}) \tag{6} \]

where \(\phi\) is the wall yielding coefﬁcient, sometimes referred to as wall extensibility (m Pa^{–1} s^{–1}) and \(P_{th}\) is threshold turgor pressure or yield threshold (\(P_{th}\)) above which the cell wall yields. The other terms are defined as before. It is obvious in Eq. 6 that \(P\) must be above \(P_{th}\) in order for the cell to enlarge. Also, as \(\phi\) becomes larger, the cell grows faster.

In tissues instead of individual cells, a similar equation applies because all the cells enlarge in concert. The enlargement of the whole organ is then described by:

\[\frac{dV}{dt} = m (P - P_{th}) \tag{7} \]

where everything is the same as in Eq. 6 except that \(m\) contains the wall yielding attributes for all the enlarging cells as well as the \(A\) term. Examples where this equation applies would be tissues of enlarging stem and root tips, hypocotyls and coleoptiles of geminating seeds, flower buds, and even growing fruits (grapes, tomatoes, maize kernels, etc).

Nevertheless, the inability of \(P\) to build enough for equilibration keeps the cell water potential lower than it otherwise would be. As a result the yielding walls create a lower water potential that is called “growth-induced” because mature cells that do not have such yielding walls (Figure 7.25). The growth-induced \(\Psi\) can move water from the mature cells into the elongating ones if no external supply is available. This probably explains how a stored potato can sprout in a cupboard because the cells in the bud develop yielding walls that create a growth-induced \(\Psi\) that moves water from the mature cells into the sprouts.

Usually the water source is in the soil or xylem (\(\Psi_o\)), and a slight modification to Eq. 5 can show this effect:

\[\frac{dV}{dt} = L (\Psi_o - \Psi_{growth-induced}) \tag{8} \]

Because the cells with yielding walls have turgor that is \(P = \Pi + \Psi_{growth-induced}\) (remember \(\Psi\) is negative), Eq. 7 becomes:

\[\frac{dV}{dt} = m (\Pi + \Psi_{growth-induced} - P_{th}) \tag{9} \]

and solving for \(\Psi_{growth-induced}\) in Eqs 8 and 9 gives:

\[\frac{dV}{dt} = \frac{mL}{m + L} (\Psi_o + \Pi - P_{th}) \tag{10} \]

This shows that growth depends on a water supply function (Eq. 8) and a water demand function (Eq. 7) that can be combined to give Eq. 10. A quick look at this latter expression shows that the growth rate of an organ is determined by the water potential of the supply, the osmotic effect of the solute minus the threshold turgor (which is too low to contribute to the growth rate) multiplied by a coefficient. In other words, the difference in water potential that we’ve seen before in Eq. 5 diminished by the threshold turgor that is inactive in the growth process provides the driving force for growth. When multiplied by the coefficient, \(\frac{mL}{m + L}\), the equation gives the growth rate of the organ.

The reason Eq. 10 is important is that it shows a plant organ grows not only because of the turgor properties of the tissue but also because water moves through all the small cells (\(L\)) of the entire organ. Meristems have dividing cells that are necessarily small. There are many wall and membrane barriers to traverse before water reaches all of the cells and allows them to grow simultaneously at a similar rate. The yielding of the walls controls the growth-induced \(\Psi\) needed for this water. In effect the turgor must be high enough for the walls to yield but low enough to create the growth-induced potential to supply water to the enlarging cells. The supply is often quite far away depending on the anatomy of the meristem and enlarging tissues. Consequently, large distances may be travelled by water for growth and the anatomy plays a large part in the growth rate of the organ.It is worth looking at the coefficient a little more deeply. If the wall yields easily and m is large (say \(m\) = 10 units and \(L\) = 1 unit), the coefficient is 10/11 and the growth rate is controlled mostly by the ability of water to move into the enlarging tissues. If the reverse occurs (\(m\) = 1, \(L\) = 10), the coefficient is still 10/11 but the growth rate is controlled mostly by the yielding properties of the walls. Therefore, comparing the magnitude of \(m\) and \(L\) is the key to determining whether the demand (\(m\)) or the supply (\(L\)) function dominates the coefficient. A picture of these effects is shown in Figure 7.26 and methods are available for measuring not only \(m\) and \(L\) but also all the other terms in these equations (Boyer et al., 1985).